Calixporphyrin - A new type of porphyrinoid container molecule

Synlett

Volumn , Issue SPEC. ISS., 1999, Pages 969-971

  Schlögl, Johann ^a   Kräutler, Bernhard ^a  

^a UNIVERSITY OF INNSBRUCK   (Austria)

Author keywords

Calixporphyrin; Container molecule; D(4h) symmetry; Host molecule; Porphyrin

Indexed keywords

ANTHRACENE; CALIXPORPHYRIN; PORPHYRIN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; GEOMETRY; MOLECULAR MODEL; REACTION ANALYSIS; SYNTHESIS;

EID: 0040138040     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3097     Document Type: Article

References (22)

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8. In analogy to the situation of "calixarenes", the name "calixporphyrin" is meant to point to the rigid, biconcave frame of 1 and to indicate the potential ability to accommodate various guest molecules (see Gutsche, C. D. Calixarenes; The Royal Society of Chemistry: Cambridge, 1992). Differing from 1, in "calixarene-porphyrins" a calixarene moiety is bound covalently to the porphyrin (e.g. Nagasaki, T.; Fujishima, H.; Takeuchi, M.; Shinkai, S. J. Chem. Soc., Perkin Trans. 1 1995, 1883).
9. In analogy to the situation of "calixarenes", the name "calixporphyrin" is meant to point to the rigid, biconcave frame of 1 and to indicate the potential ability to accommodate various guest molecules (see Gutsche, C. D. Calixarenes; The Royal Society of Chemistry: Cambridge, 1992). Differing from 1, in "calixarene-porphyrins" a calixarene moiety is bound covalently to the porphyrin (e.g. Nagasaki, T.; Fujishima, H.; Takeuchi, M.; Shinkai, S. J. Chem. Soc., Perkin Trans. 1 1995, 1883).
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17. 4.
18. Molecular modeling calculations have been performed using SYBYL software (Version 6.3 A) using the forcefield provided by Tripos Associates, St. Louis MO.
19. 0 is the concentration of the amine). (table presented)
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